ALBERT

Description: From December 1986 until April 1987 ground-based microwave observations of the diurnal variation of mesospheric ozone were made over Bern, Switzerland. These data were of sufficient quality to define the characteristics diurnal behavior of the ozone mixing ratio during winter and equinoctial conditions. The observed diurnal variation of ozone peaks at about 74 km, where its amplitude is about a factor of 6. At 65 km the observed diurnal variation is a factor of 3, whereas at 55 km it is only a factor of 1.4. One-dimensional model calculations accurately reproduce the relative diurnal variation of ozone at equinox, suggesting that the model value of the ozone photolysis rate coefficient is accurate to better that 10 percent. For winter conditions, however, the model underpredicts the observed relative diurnal variation by a factor of 2; a major part of this discrepancy is due to an observed postmidnight increase in ozone. Various suggested changes in model parameters to better produce the ozone abundance vertical profile result in only small differences in the relative diurnal variation, indicating that these observations do not provide a sensitive test of the mesospheric chemistry controlling the abundance of odd oxygen.

Description: Ground-based spectral line measurements of the 22.2 GHz water vapor line in atmospheric emission were made at the Jet Propulsion Laboratory, which have been used to deduce the mesospheric water vapor profile. The measurements were made nearly continuously in the spring and early summer of 1984. The results indicate a temporal increase in the water vapor mixing ratio in the upper mesosphere from April through June. At 75 km, this increase is nearly by a factor of 2. Comparison of the present results with the results of a similar series of measurements made at the Haystack (radio astronomy) Observatory indicate that this temporal increase is part of a seasonal variation.

Description: An investigation is conducted in order to determine the relative importance of several modeled processes in controlling the magnitude and phase of the mesospheric ozone response. A detailed one-dimensional modeling study of the mesospheric ozone response to solar UV flux variations is conducted to remove some of the deficiencies in previous studies. This study is also used to examine specifically the importance of solar zenith angle, self-consistent calculation of water vapor abundance, and temperature feedback with a nonlocal thermodynamic equilibrium radiation model. The photochemical model is described, and the assumptions made for the purpose of comparing model results with the observed ozone response obtained from a statistical analysis of Solar Mesosphere Explorer data (Keating et al., 1987) are discussed. The numerical results for the theoretical ozone response are presented. The results of selected time-dependent calculations are considered to illustrate the degree to which a relatively simple model of the mesosphere is able to capture the major characteristics of the observed response.

Description: Ground-based spectral line measurements of the 22.2 GHz atmospheric water vapor line in emission were made at the JPL in order to obtain data in a dry climate, and to confirm similar measurements made at the Haystack Observatory. The results obtained from March 1984 to July 1984 and from December 1984 to May 1985, were based on data recorded by a HP9816 microcomputer. The instrument spectrometer was a 64 channel, 62.5 kHz resolution filter bank. Data indicates the existence of a seasonal variation in the abundance of water vapor in the upper mesosphere, with mixing ratios higher in summer than in spring. This is consistent with recent theoretical and observational results. In the area of semiannual oscillation, Haystack data are more consistent than those of JPL, indicating an annual cycle with abundances at maximum in summer and minimum in winter.

Description: We report on stratospheric and mesospheric water vapor (H2O) observations obtained by the Millimeter wave Atmospheric Sounder (MAS) in the Arctic spring of 1992. In the lower stratosphere, the observations show enhanced H2O inside the vortex between 450 K and 625 K, in agreement with other H2O observations. In the upper stratosphere and lower mesosphere, at potential temperatures between 1850 K and 2200 K, we find regions of depressed H2O volume mixing ratio coincident with remnants of high potential vorticity. The depressed mesospheric H2O, as well as the enhanced lower stratospheric H2O, are consistent with wintertime descent. It also suggests effective containment of air up into the lower mesosphere.

Description: Latitudinal distributions of upper stratospheric ClO measured by MAS during the three ATLAS missions are presented for northern hemisphere (NH) spring equinox in 1992, southern hemisphere (SH) early fall in 1993, and NH fall in 1994. The MAS ClO results are shown along with correlative MLS observations. The results of both instruments consistently show the same latitudinal features. The ClO maximum in the NH spring occurs at mid latitudes, whereas the latitudinal ClO maximum in both the NH and SH fall occurs at high latitudes. The volume mixing ratio maxima were significantly higher in the fall (0.7-0.8 ppbv) than in spring (0.5-0.6 ppbv). Qualitatively, these results are consistent with calculations of several 2-D models.

Description: Ozone profile measurements were made by three instruments, ATMOS, MAS, and SSBUV, using distinctly different observing techniques, as part of the ATLAS Space Shuttle missions in March 1992, April 1993, and November 1994. ATMOS makes solar-occultation observations of infrared spectra using a Fourier transform interferometer. MAS uses a limb-scanning antenna to measure emission spectra at millimeter wavelengths. SSBUV is a nadir-viewing instrument measuring the transmission of scattered solar ultraviolet radiation modified by ozone absorption. A sample of zonal-mean mixing ratio profiles indicates that these three ATLAS instruments generally agree to within 10%, although a few potential biases have been noted. There are significant differences in the character of the agreement between ATLAS 1 and ATLAS 2 which will require further study.

Description: We compared the version 5 Microwave Limb Sounder (MLS) aboard the Upper Atmosphere Research Satellite (UARS), version 3 Polar Ozone and Aerosol Measurement-III (POAM-111) aboard the French satellite SPOT-IV, version 6.0 Stratospheric Aerosol and Gas Experiment 11 (SAGE-II) aboard the Earth Radiation Budget Satellite, and NASA ER-2 aircraft measurements made in the northern hemisphere in January-February 2000 during the SAGE III Ozone Loss and Validation Experiment (SOLVE). This study addresses one of the key scientific objectives of the SOLVE campaign, namely, to validate multi-platform satellite measurements made in the polar stratosphere during winter. This intercomparison was performed using a traditional correlative analysis (TCA) and a trajectory hunting technique (THT). Launching backward and forward trajectories from the points of measurement, the THT identifies air parcels sampled at least twice within a prescribed match criterion during the course of 5 days. We found that the ozone measurements made by these four instruments agree most of the time within 110% in the stratosphere up to 1400 K (approximately 35 km). The water vapor measurements from POAM-III and the ER-2 Harvard Lyman-alpha hygrometer and JPL laser hygrometer agree to within 10.5 ppmv (or about +/-10%) in the lower stratosphere above 380 K. The MLS and ER-2 ClO measurements agree within their error bars for the TCA. The MLS and ER-2 nitric acid measurements near 17-20 km altitude agree within their uncertainties most of the time with a hint of a positive offset by MLS according to the TCA. We also applied the AER box model constrained by the ER-2 measurements for analysis of the ClO and HN03 measurements using the THT. We found that: (1) the model values of ClO are smaller by about 0.3-0.4 (0.2) ppbv below (above) 400 K than those by MLS and (2) the HN03 comparison shows a positive offset of MLS values by approximately 1 and 1-2 ppbv below 400 K and near 450 K, respectively. It is hard to quantify the HN03 offset in the 400-440 K range because of the high sensitivity of nitric acid to the PSC schemes. Our study shows that, with some limitations (like HN03 comparison under PSC conditions), the THT is a more powerful tool for validation studies than the TCA, making conclusions of the comparison statistically more robust.